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Fabrication of β-CoVO nanorods embedded in graphene sheets and their application for electrochemical charge storage electrode.

作者信息

Jeong Gyoung Hwa, Lee Ilbok, Lee Donghyun, Lee Hea-Min, Baek Seungmin, Kwon O-Pil, Kumta Prashant N, Yoon Songhun, Kim Sang-Wook

机构信息

Department of Chemistry, Ulsan National Institute of Science and Technology (UNIST), 50, Unist-gil, Ulsan 44919, Republic of Korea.

出版信息

Nanotechnology. 2018 May 11;29(19):195403. doi: 10.1088/1361-6528/aaae3e. Epub 2018 Feb 9.

Abstract

The fabrication of β-CoVO nanorods embedded in graphene sheets and their application as electrochemical charge storage electrodes is reported. From the surfactant treatment of raw graphite, graphene was directly prepared and its nanocomposite with β-CoVO nanorods distributed between graphene layers (β-CoVO-G) was synthesized by a hydrothermal method. When applied as an anode in lithium-ion batteries, the β-CoVO-G anode exhibits greatly improved charge and discharge capacities of 790 and 627 mAh · g, respectively, with unexpectedly high initial efficiency of 82%. The observed discharge capacity reflected that at least 3.7 mol of Li is selectively accumulated within the β-CoVO phase (LiCoVO, x > 3.7), indicative of significantly improved Li uptake when compared with aggregated β-CoVO nanorods. Moreover, very distinct peak plateaus and greatly advanced cycling performance are observed, showing more improved Li storage within the β-CoVO phase. As a supercapacitor electrode, moreover, our composite electrode exhibits very high peak pseudocapacitances of 2.71 F · cm and 433.65 F · g in the β-CoVO phase with extremely stable cycling performance. This remarkably enhanced performance in the individual electrochemical charge storage electrodes is attributed to the novel phase formation of β-CoVO and its optimized nanocomposite structure with graphene, which yield fast electrical conduction through graphene, easy accessibility of ions through the open multilayer nanosheet structure, and a relaxation space between the β-CoVO-G.

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